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Lineage relationship and protective immunity of memory CD8 T cell subsets
Abstract
Memory CD8 T cells can be divided into two subsets, central (T(CM)) and effector (T(EM)), but their lineage relationships and their ability to persist and confer protective immunity are not well understood. Our results show that T(CM) have a greater capacity than T(EM) to persist in vivo and are more efficient in mediating protective immunity because of their increased proliferative potential. We also demonstrate that, following antigen clearance, T(EM) convert to T(CM) and that the duration of this differentiation is programmed within the first week after immunization. We propose that T(CM) and T(EM) do not necessarily represent distinct subsets, but are part of a continuum in a linear naive --> effector --> T(EM) --> T(CM) differentiation pathway.
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“the central memory (CM) or effector memory (EM) differentiation states of CD4+ and CD8+ T cells have implications for durability, recirculation, tissue access, and responses upon antigen re-exposure (Kaech et al., 2002; Martin and Badovinac, 2018; Wherry et al., 2003).”
From Rapid induction of antigen-specific CD4+ T cells is associated with coordinated humoral and cellular immunity to SARS-CoV-2 mRNA vaccination (2021) · cites this paper as Wherry et al., 2003
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Metadata
- Authors
- Wherry, E. J., Teichgräber, V., Becker, T. C., Masopust, D., Kaech, S. M., Antia, R., von Andrian, U. H., & Ahmed, R.
- Affiliations
- Emory University (US)
- Corresponding author
- Ahmed, Rafi
- Venue
- Nature Immunology
- Published
- 2003-02-03
- Volume
- 4
- Issue
- 3
- Pages
- 225-234
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- OpenAlex
- W2029128444
- Cited by
- 1,864
- References
- 57
- Citations by year
- 2026: 27 · 2025: 44 · 2024: 47 · 2023: 55 · 2022: 61 · 2021: 65 · 2020: 59 · 2019: 59 · 2018: 54 · 2017: 60 · 2016: 68 · 2015: 50 · 2014: 74 · 2013: 92 · 2012: 84
- FWCI
- 47.89
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (T32GM008169)
- National Institute of Allergy and Infectious Diseases (AI44644, AI 30048)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Keywords
- memory CD8+ T cells, central memory T cells, effector memory T cells, T cell lineage, T cell differentiation, T cell proliferation, protective immunity, antigen clearance, naive T cells, T cell persistence
- MeSH terms
- Animals, Cell Communication, Cell Division, Immunologic Memory, Listeriosis, Listeria monocytogenes, Lymphocytic Choriomeningitis, Lymphocytic choriomeningitis virus, Mice, Transgenic, CD8-Positive T-Lymphocytes, Cell Lineage, Mice
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